Citramon
NDC Package 16638-118-13

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Citramon is adults and children over 15 years take 1 tablet 2 - 3 times a day. Marketed by Borisovskiy Zavod Medicinskikh Preparatov Jsc, this product is identified by NDC 16638-118 and is authorized under FDA application part343.

Identification & Billing

NDC Package Code
16638-118-13
Package Description
3300 mg in 1 PACKAGE
Product Code
11-Digit Billing Format
16638011813
RxNorm Crosswalk
  • RxCUI: 1673788 - acetaminophen 200 MG / aspirin 220 MG / caffeine 27 MG Oral Tablet
  • RxCUI: 1673788 - APAP 200 MG / ASA 220 MG / Caffeine 27 MG Oral Tablet

Clinical Specifications

Proprietary Name
Citramon
Dosage Form
-
Usage Information
Adults and children over 15 years take 1 tablet 2 - 3 times a day. The interval between the drug intakes should be at least 6 - 8 hours. Maximum single dose is 2 tablets, maximum daily dose is 4 tablets.

Regulatory & Marketing

Labeler Name
Borisovskiy Zavod Medicinskikh Preparatov Jsc
FDA Application #
part343
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
06-26-1996
Listing Expiration
12-31-2017
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 16638-118-13 identifies a specific commercial package of 3300 mg in 1 package of Citramon, labeled by Borisovskiy Zavod Medicinskikh Preparatov Jsc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Borisovskiy Zavod Medicinskikh Preparatov Jsc on June 26, 1996. The current certification is valid through December 31, 2017.

How is this Borisovskiy Zavod Medicinskikh Preparatov Jsc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 16638011813. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
16638-118-13
11-Digit CMS (5-4-2)
16638-0118-13

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.